NDC 76335-003

SP6 Complete

Abies Canadensis, Ammonium Bromatum, Ammonium Muriaticum, Anaradium Orientale, Antimonium Crudum, Argentum Metallicum, Calcarea Carbonica, Capsicum, Cinchona, Ferrum Metallicum, Fucus, Ignatia, Kali Bichromicum, Natrum Sulphuricum, Oleander, Phosphorus, Phytolacca, Sabadilla, Staphysagria, Sulphur, Thyroidinum, Veratrum Album

SP6 Complete is a Topical Patch in the Human Otc Drug category. It is labeled and distributed by Lifewave, Inc.. The primary component is Tsuga Canadensis Bark; Ammonium Bromide; Ammonium Chloride; Semecarpus Anacardium Juice; Antimony Trisulfide; Silver; Oyster Shell Calcium Carbonate, Crude; Capsicum; Cinchona Officinalis Bark; Iron; Fucus Vesiculosus; Strychnos Ignatii Seed; Potassium Dichromate; Sodium Sulfate; Nerium Oleander Leaf; Phosphorus; Phytolacca Americana Root; Schoenocaulon Officinale Seed; Delphinium Staphisagria Seed; Sulfur; Thyroid, Unspecified; Veratrum Album Root.

Product ID76335-003_ad893816-b204-4661-8ad3-009d6bda7d8c
NDC76335-003
Product TypeHuman Otc Drug
Proprietary NameSP6 Complete
Generic NameAbies Canadensis, Ammonium Bromatum, Ammonium Muriaticum, Anaradium Orientale, Antimonium Crudum, Argentum Metallicum, Calcarea Carbonica, Capsicum, Cinchona, Ferrum Metallicum, Fucus, Ignatia, Kali Bichromicum, Natrum Sulphuricum, Oleander, Phosphorus, Phytolacca, Sabadilla, Staphysagria, Sulphur, Thyroidinum, Veratrum Album
Dosage FormPatch
Route of AdministrationTOPICAL
Marketing Start Date2009-12-31
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameLifewave, Inc.
Substance NameTSUGA CANADENSIS BARK; AMMONIUM BROMIDE; AMMONIUM CHLORIDE; SEMECARPUS ANACARDIUM JUICE; ANTIMONY TRISULFIDE; SILVER; OYSTER SHELL CALCIUM CARBONATE, CRUDE; CAPSICUM; CINCHONA OFFICINALIS BARK; IRON; FUCUS VESICULOSUS; STRYCHNOS IGNATII SEED; POTASSIUM DICHROMATE; SODIUM SULFATE; NERIUM OLEANDER LEAF; PHOSPHORUS; PHYTOLACCA AMERICANA ROOT; SCHOENOCAULON OFFICINALE SEED; DELPHINIUM STAPHISAGRIA SEED; SULFUR; THYROID, UNSPECIFIED; VERATRUM ALBUM ROOT
Active Ingredient Strength10 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 76335-003-30

30 PATCH in 1 BOX (76335-003-30)
Marketing Start Date2009-12-31
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 76335-003-30 [76335000330]

SP6 Complete PATCH
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-12-31
Inactivation Date2020-01-31

Drug Details


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